학술논문
Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort
Document Type
Article
Author
Dias, K.-R.; Evans, C.-A.; Zhu, Y.; Zhang, F.; Roscioli, T.; Shrestha, R.; Schofield, D.; Standen, K.; Lucas, C.; Carey, L.; Cliffe, C.; Elakis, G.; Kirk, E.P.; Fletcher, J.; Walsh, R.; Buckley, M.F.; O'Heir, E.; Weisburd, B.; Stenton, S.L.; Sanchis-Juan, A.; Brand, H.; Talkowski, M.E.; O'Donnell-Luria, A.; Dudding-Byth, T.; Field, M.; Ma, A.; Wilson, M.; Sandaradura, S.A.; Smith, J.; Adès, L.C.; Ghedia, S.; Kamien, B.; Turner, A.; Mowat, D.; Ewans, L.J.; Bakshi, M.; Regan, M.; Krzesinski, E.; Hunter, M.F.; Fennell, A.P.; McGillivray, G.; Savarirayan, R.; White, S.M.; Tan, T.Y.; Stark, Z.; Brown, N.J.; Yeung, A.; Wall, M.; Lunke, S.; Boughtwood, T.; North, K.; Amor, D.J.; Pérez-Jurado, L.A.; Akesson, L.; Rapadas, M.; Stevanovski, I.; Deveson, I.W.; Kerkhof, J.; Sadikovic, B.; French, H.; Corbett, M.A.; Kroes, T.; Gecz, J.; Meldrum, C.; Cliffe, S.
Source
In: Genetics in Medicine . (Genetics in Medicine, May 2024, 26(5))
Subject
Language
English
ISSN
15300366
10983600
10983600